Effect of ANNE One-Wellue Device Array Use on Staff Bedside Vital Sign Measurement Activity
Purpose
Randomized controlled trial of a time motion study of time spent obtaining and charting vital signs for inpatients, comparing use of a wireless Bluetooth vital sign array as intervention versus routine vital sign obtainment activity on a general medical floor.
Conditions
- Vital Sign Evaluation
- Vital Sign Monitoring
- Sleep Quality
- Provider Behavior
- Patient Satisfaction
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Genders
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Inpatients admitted to Northwestern Memorial Hospital, Feinberg Unit 16 West.
Exclusion Criteria
- Primary language other than English, under isolation status, pregnant patients, prisoners, employees or students of the hospital or Northwestern University.
Study Design
- Phase
- N/A
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel Assignment
- Intervention Model Description
- Randomized Controlled Trial
- Primary Purpose
- Health Services Research
- Masking
- None (Open Label)
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Experimental Intervention--Device Array Use |
Inpatients will wear the ANNE One device array for obtainment of vital sign assessments. |
|
|
Active Comparator Control--Routine Vital Sign Obtainment |
Inpatients will have vital signs determined by routine practice, using any other standard of care-accepted method or device. |
|
Recruiting Locations
Feinberg 16 West, Northwestern Memorial Hospital
Chicago, Illinois 60611
Chicago, Illinois 60611
More Details
- NCT ID
- NCT06995742
- Status
- Recruiting
- Sponsor
- Northwestern University